<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Rokoff LB</submitter><funding>ACL HHS</funding><funding>NIEHS NIH HHS</funding><funding>NIOSH CDC HHS</funding><pagination>112701</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8917058</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>208</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Although prenatal chemical exposures influence neurobehavior, joint exposures are not well explored as risk factors for internalizing disorders through adolescence.&lt;h4>Objective&lt;/h4>To evaluate associations of prenatal organochlorine and metal exposures, considered individually and as a mixture, with mid-childhood and adolescent internalizing symptoms.&lt;h4>Methods&lt;/h4>Participants were 468 children from a prospective cohort recruited at birth (1993-1998) in New Bedford, Massachusetts. Organochlorines (hexachlorobenzene, p,p'-dichlorodiphenyl dichloroethylene, polychlorinated biphenyls) and metals (lead, manganese) were analyzed in cord blood. Internalizing symptoms (anxiety, depressive, somatic) were assessed via multiple informants on the Conners' Rating Scale (CRS) at 8-years and Behavior Assessment System for Children, Second Edition (BASC-2) at 15-years; higher T-scores indicate greater symptoms. Overall and sex-specific covariate-adjusted associations were evaluated using Bayesian Kernel Machine Regression (BKMR) and five-chemical linear regression models.&lt;h4>Results&lt;/h4>The cohort was socioeconomically diverse (35% household income &lt;$20,000; 55% maternal ≤ high school education at birth). Most chemical concentrations were consistent with background levels [e.g., median (range) cord blood lead: 1.1 (0-9.4) μg/dL]. BKMR suggested linear associations and no interactions between chemicals. The overall mixture was positively associated with Conners' Parent Rating Scale (CPRS) and BASC-2 Self Report of Personality (SRP) anxiety and depressive symptoms, and negatively with somatic symptoms. Prenatal lead was positively associated with adolescent anxiety symptoms [1.56 (95% CI: 0.50, 2.61) BASC-2 SRP Anxiety score increase per doubling lead]. For CRPS and BASC-2 SRP, a doubling of cord blood manganese was positively associated with internalizing symptoms for girls [e.g., 3.26 (95% CI: 0.27, 6.25) BASC-2 SRP Depression score increase], but not boys. Organochlorine exposures were not adversely associated with internalizing symptoms.&lt;h4>Discussion&lt;/h4>Low-level prenatal lead exposure was positively associated with adolescent anxiety symptoms, and prenatal manganese exposure was positively associated with internalizing symptoms for girls from mid-childhood through adolescence. In utero neurotoxicant metal exposures may contribute to the emergence of anxiety and depression.</pubmed_abstract><journal>Environmental research</journal><pubmed_title>Prenatal exposure to a mixture of organochlorines and metals and internalizing symptoms in childhood and adolescence.</pubmed_title><pmcid>PMC8917058</pmcid><funding_grant_id>R01 ES014864</funding_grant_id><funding_grant_id>T42 OH008416</funding_grant_id><funding_grant_id>P30 ES000002</funding_grant_id><funding_grant_id>T42OH008416</funding_grant_id><funding_grant_id>P42 ES005947</funding_grant_id><pubmed_authors>Shoaff JR</pubmed_authors><pubmed_authors>Bellinger DC</pubmed_authors><pubmed_authors>Enlow MB</pubmed_authors><pubmed_authors>Coull BA</pubmed_authors><pubmed_authors>Rokoff LB</pubmed_authors><pubmed_authors>Korrick SA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Prenatal exposure to a mixture of organochlorines and metals and internalizing symptoms in childhood and adolescence.</name><description>&lt;h4>Background&lt;/h4>Although prenatal chemical exposures influence neurobehavior, joint exposures are not well explored as risk factors for internalizing disorders through adolescence.&lt;h4>Objective&lt;/h4>To evaluate associations of prenatal organochlorine and metal exposures, considered individually and as a mixture, with mid-childhood and adolescent internalizing symptoms.&lt;h4>Methods&lt;/h4>Participants were 468 children from a prospective cohort recruited at birth (1993-1998) in New Bedford, Massachusetts. Organochlorines (hexachlorobenzene, p,p'-dichlorodiphenyl dichloroethylene, polychlorinated biphenyls) and metals (lead, manganese) were analyzed in cord blood. Internalizing symptoms (anxiety, depressive, somatic) were assessed via multiple informants on the Conners' Rating Scale (CRS) at 8-years and Behavior Assessment System for Children, Second Edition (BASC-2) at 15-years; higher T-scores indicate greater symptoms. Overall and sex-specific covariate-adjusted associations were evaluated using Bayesian Kernel Machine Regression (BKMR) and five-chemical linear regression models.&lt;h4>Results&lt;/h4>The cohort was socioeconomically diverse (35% household income &lt;$20,000; 55% maternal ≤ high school education at birth). Most chemical concentrations were consistent with background levels [e.g., median (range) cord blood lead: 1.1 (0-9.4) μg/dL]. BKMR suggested linear associations and no interactions between chemicals. The overall mixture was positively associated with Conners' Parent Rating Scale (CPRS) and BASC-2 Self Report of Personality (SRP) anxiety and depressive symptoms, and negatively with somatic symptoms. Prenatal lead was positively associated with adolescent anxiety symptoms [1.56 (95% CI: 0.50, 2.61) BASC-2 SRP Anxiety score increase per doubling lead]. For CRPS and BASC-2 SRP, a doubling of cord blood manganese was positively associated with internalizing symptoms for girls [e.g., 3.26 (95% CI: 0.27, 6.25) BASC-2 SRP Depression score increase], but not boys. Organochlorine exposures were not adversely associated with internalizing symptoms.&lt;h4>Discussion&lt;/h4>Low-level prenatal lead exposure was positively associated with adolescent anxiety symptoms, and prenatal manganese exposure was positively associated with internalizing symptoms for girls from mid-childhood through adolescence. In utero neurotoxicant metal exposures may contribute to the emergence of anxiety and depression.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 May</publication><modification>2025-04-19T13:29:51.859Z</modification><creation>2025-04-19T13:29:51.859Z</creation></dates><accession>S-EPMC8917058</accession><cross_references><pubmed>35016863</pubmed><doi>10.1016/j.envres.2022.112701</doi></cross_references></HashMap>